DisGeNET

DisGeNET is a knowledge management platform that integrates and standardizes the data of genes and mutations related to diseases from multiple sources. It covers entire range of human disease.

Source Last Updated
DisGeNET July 29, 2024
Displaying entries 9326 - 9350 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name UniProt ID ▲
C0024117 Chronic Obstructive Airway Disease PRNP 5621 prion protein P04156
C0032002 Pituitary Diseases PRNP 5621 prion protein P04156
C0003850 Arteriosclerosis PRNP 5621 prion protein P04156
C0149931 Migraine Disorders PRNP 5621 prion protein P04156
C1861736 SPINOCEREBELLAR ATAXIA 31 (disorder) PRNP 5621 prion protein P04156
C0031069 Familial Mediterranean Fever PRNP 5621 prion protein P04156
C0205710 Alpers Syndrome (disorder) PRNP 5621 prion protein P04156
C1306600 Radial nerve palsy PRNP 5621 prion protein P04156
C1708349 Hereditary Diffuse Gastric Cancer PRNP 5621 prion protein P04156
C1854520 SEBASTIAN SYNDROME PRNP 5621 prion protein P04156
C0017601 Glaucoma PRNP 5621 prion protein P04156
C0001889 Akinetic Mutism PRNP 5621 prion protein P04156
C0002895 Anemia, Sickle Cell PRNP 5621 prion protein P04156
C0027051 Myocardial Infarction PRNP 5621 prion protein P04156
C0028738 Nystagmus PRNP 5621 prion protein P04156
C0038454 Cerebrovascular accident PRNP 5621 prion protein P04156
C1332986 Childhood Osteosarcoma PRNP 5621 prion protein P04156
C0162311 Androgenetic Alopecia PRNP 5621 prion protein P04156
C0017609 Glaucoma, Neovascular PRNP 5621 prion protein P04156
C0009806 Constipation PRNP 5621 prion protein P04156
C1969957 Creutzfeldt-Jakob Disease, Heidenhain Variant PRNP 5621 prion protein P04156
C0002170 Alopecia PRNP 5621 prion protein P04156
C0751772 REM Sleep Behavior Disorder PRNP 5621 prion protein P04156
C4083212 Alopecia, Male Pattern PRNP 5621 prion protein P04156
C0003850 Arteriosclerosis LCAT 3931 lecithin-cholesterol acyltransferase P04180

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Last updated: August 19, 2024